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| created at |
2021-12-22 03:08:20 UTC |
| updated at |
2021-12-22 07:06:09 UTC |
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MONDO_bioport_pref_name
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183,974 entries
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There is 0 pattern entry.
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partial deletion of chromosome type 16
|
16878 |
|
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uterine corpus mullerian adenosarcoma
|
2878 |
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malignant melanoma of choroid
|
3878 |
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melanoma (disease) of optic choroid
|
3878 |
|
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partial deletion of chromosome 16
|
16878 |
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partial monosomy of chromosome 16
|
16878 |
|
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malignant melanoma of the choroid
|
3878 |
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autosomal dominant osteosclerosis
|
11878 |
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Atrophies, hereditary optic
|
43878 |
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atrophy, hereditary optic
|
43878 |
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Mullerian adenosarcoma of the uterus
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2878 |
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acquired gastric outlet stenosis
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1878 |
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PROP1 combined pituitary hormone deficiencies, genetic form
|
9878 |
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hereditary spastic paraplegia 6
|
10878 |
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familial spastic paraplegia autosomal dominant 3
|
10878 |
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